Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Neutrophil elastase gene variation and coronary heart disease.

Pharmacogenetics and genomics - 1 Aug 2007

Schönfelder Jacqueline, Telgmann Ralph, Nicaud Viviane, Brand Eva, Dördelmann Corinna, Rüssmann Christina, Beining Katrin, Schmidt-Petersen Klaus, Evans Alun, Kee Frank, Morrison Caroline, Arveiler Dominique, Cambien François, Paul Martin, Brand-Herrmann Stefan-Martin

Abstract excerpt

AIMS: Identification and functional characterization of variants in the neutrophil elastase (ELA2) gene in cardiovascular disease. METHODS: From participants of the ECTIM (Etude Cas-Témoins sur l'infarctus du Myocarde) Study with myocardial infarction (MI) 2082 chromosomes were genetically scanned; 990 patients with MI and 904 controls were genotyped for the common polymorphisms G-761A and S173S (C4890A)....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acid Substitution
Share to Base Pairing

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Coronary Disease

Share to Leukocyte Elastase

Share to Myocardial Infarction

Share to Promoter Regions, Genetic

Share to RNA Stability

Share to Sequence Deletion

Source

Identifiers

PMID: 17622939
DOI: 10.1097/FPC.0b013e328042bb46

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Neutrophil elastase gene variation and coronary heart disease.PMID 17622939Read ↗

Risk of coronary artery disease as influenced by variants of the human endothelin and endothelin-converting enzyme genes.Semantic proximity Read ↗

Polymorphisms of the endothelial nitric oxide synthase gene - no consistent association with myocardial infarction in the ECTIM study.Semantic proximity Read ↗

Polymorphisms of the endothelin-A and -B receptor genes in relation to blood pressure and myocardial infarction The etude cas-témoins sur l'infarctus du myocarde (ECTIM) studySemantic proximity Read ↗

Lack of association between endothelin-1 gene variants and myocardial infarction.Semantic proximity Read ↗

Polymorphisms of the P-selectin gene and risk of myocardial infarction in men and women in the ECTIM extension study. Etude cas-temoin de l'infarctus myocarde.Semantic proximity Read ↗

Lipid-related genes and myocardial infarction in 4685 cases and 3460 controls: discrepancies between genotype, blood lipid concentrations, and coronary disease risk.Semantic proximity Read ↗

New polymorphisms of the angiotensin II type 1 receptor gene and their associations with myocardial infarction and blood pressure: the ECTIM study. Etude Cas-Témoin de l'Infarctus du Myocarde.Semantic proximity Read ↗

No large-effect low-frequency coding variation found for myocardial infarction.Semantic proximity Read ↗

Analysis of Matrix Metalloproteinase-8 Gene Polymorphisms and Their Association with Long-Term Survival, Clinical Phenotype, and Disease Risk in Patients with Coronary Artery Disease.Semantic proximity Read ↗

Apolipoprotein B signal peptide polymorphism in patients with myocardial infarction and controls. "The ECTIM study".Semantic proximity Read ↗

Angiotensin II type-I receptor and ACE polymorphisms and risk of myocardial infarction in men and women.Semantic proximity Read ↗

Identification of two polymorphisms in the early growth response protein-1 gene: possible association with lipid variables.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.